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T.ELONGATUS ndh (data-set 1)

Analyse T.ELONGATUS ndh (data-set 1) in the GL1X research workbench: secondary structure, accessibility, pockets, interfaces, conservation, variants, modifications, peptides, crosslinks and neighbours on the 3D structure.

PDB
6NBQ
Type
protein
Length
3,755 residues
Chains
17
Method
electron microscopy
Collection
MolNFT v1 / PDB
Contract
0xDE3723766Bc32dcACD03C17BaA400A7B36837Eba
Owner
0x3396CDB397284571d12822B4ae1189a8E22AAAAA
Molecule
NAD(P)H-quinone oxidoreductase subunit H; NAD(P)H-quinone oxidoreductase subunit J…
EC
1.6.5.-, 7.1.1.-, 1.6.5.11
UniProt
Q8DJD9, Q8DJ01, Q8DKZ4, Q8DL31, Q8DJU2, Q8DKZ3, Q8DLN5, Q8DMU4, Q8DL61, Q8DJ02, Q8DL29, V5V507, Q8DKX9, Q8DKY0, Q8DMR6, Q8DL30
Ligands
SF4
Pockets
20 · best druggability 0.86

Structure

electron microscopy · 17 distinct chains · 50% helix, 7% strand (DSSP).

ChainMoleculeTypeResiduesSecondary structureUniProt
HNAD(P)H-quinone oxidoreductase subunit H (EC 1.6.5.-)protein39242% helix, 13% strandQ8DJD9
JNAD(P)H-quinone oxidoreductase subunit J (EC 1.6.5.-)protein16119% helix, 25% strandQ8DJ01
KNAD(P)H-quinone oxidoreductase subunit K (EC 1.6.5.-)protein21229% helix, 10% strandQ8DKZ4
INAD(P)H-quinone oxidoreductase subunit I (EC 1.6.5.-)protein18421% helix, 10% strandQ8DL31
NNAD(P)H-quinone oxidoreductase subunit N (EC 1.6.5.-)protein14828% helix, 20% strandQ8DJU2
LNAD(P)H-quinone oxidoreductase subunit L (EC 1.6.5.-)protein6652% helix, 0% strandQ8DKZ3
MNAD(P)H-quinone oxidoreductase subunit M (EC 1.6.5.-)protein11133% helix, 26% strandQ8DLN5
ONAD(P)H-quinone oxidoreductase subunit O (EC 1.6.5.-)protein6916% helix, 33% strandQ8DMU4
STLR0636 proteinprotein570% helix, 37% strandQ8DL61
ANdhaprotein35954% helix, 0% strand—
CNAD(P)H-quinone oxidoreductase subunit 3 (EC 7.1.1.-)protein9371% helix, 0% strandQ8DJ02
ENAD(P)H-quinone oxidoreductase subunit 4L (EC 1.6.5.-)protein10176% helix, 2% strandQ8DL29
PProton-translocating NADH-quinone dehydrogenase subunit P ndhpprotein4243% helix, 0% strandV5V507
FNADH dehydrogenase subunit 5protein58259% helix, 3% strandQ8DKX9
DNAD(P)H-quinone oxidoreductase chain 4 1 (EC 1.6.5.-)protein50467% helix, 1% strandQ8DKY0
BNAD(P)H-quinone oxidoreductase subunit 2 (EC 7.1.1.-)protein48367% helix, 2% strandQ8DMR6
GNADH-quinone oxidoreductase subunit J (EC 1.6.5.11)protein19153% helix, 0% strandQ8DL30

Ligands and binding sites

  • SF4 · Iron/sulfur cluster · ligand · 3 copies · chains H, K, I

Binding sites are the residues within 4.5 Å of a ligand's heavy atoms.

Pockets

20 pockets found on a 1 Å grid, 20 with a druggability of 0.5 or more.

PocketVolume (ų)DruggabilityBuriednessLining residuesInside
17320.860.8973empty
211230.850.8691empty
35760.850.9079empty
410660.820.8393empty
510230.810.82116empty

Interfaces

49 interfaces between chains.

  • E–G · 3302 Ų buried · 18 hydrogen bonds · protein-protein
  • B–G · 2560 Ų buried · 13 hydrogen bonds · protein-protein
  • F–D · 2491 Ų buried · 14 hydrogen bonds · protein-protein
  • K–M · 2433 Ų buried · 38 hydrogen bonds · protein-protein
  • C–G · 2087 Ų buried · 3 hydrogen bonds · protein-protein

Modifications

Observed in the structure: 1 disulfide (disulfide).

Compared structures

  • 6NBQ · T.elongatus NDH (data-set 1) · the same entry in another collection · chain O against O, TM-score 1.00

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